Canonical Allele Identifier: CA2804914999

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152520_80152521insG , CM000677.2:g.80152520_80152521insG	GRCh38
NC_000015.9:g.80444862_80444863insG , CM000677.1:g.80444862_80444863insG	GRCh37
NC_000015.8:g.78231917_78231918insG	NCBI36
NG_012833.1:g.4522_4523insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-55_-54insG	ENSP00000453152.1:n.-55_-54insG